403757004: Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn) (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\...

\Aplasia of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)

\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)

\General finding of soft tissue\Skin finding\Disorder of skin\Aplasia of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
\General finding of soft tissue\Skin finding\Disorder of skin\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Aplasia of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)

\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Aplasia of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
\Integumentary system finding\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
\Integumentary system finding\Skin finding\Disorder of skin\Aplasia of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
\Integumentary system finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)

\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Aplasia of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
\Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Aplasia of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)

Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

1771683015 Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn) (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

1782767017 Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn) en Synonym Active Initial character case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Associated morphology	Aplasia	true	Inferred relationship	Some	1
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Is a	4p partial monosomy syndrome	false	Inferred relationship	Some
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Is a	Aplasia cutis congenita	true	Inferred relationship	Some
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Associated morphology	Congenital absence	false	Inferred relationship	Some	1
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Finding site	Sex chromosome	false	Inferred relationship	Some
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Associated morphology	Monosomy	false	Inferred relationship	Some
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Occurrence	Congenital	false	Inferred relationship	Some
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Finding site	Chromosome pair 4	false	Inferred relationship	Some	2
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Finding site	Structure of skin region	false	Inferred relationship	Some	1
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Associated morphology	Deletion of short arm	false	Inferred relationship	Some
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	2
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Finding site	Skin structure	false	Inferred relationship	Some	1
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Associated with	4p partial monosomy syndrome	true	Inferred relationship	Some	2
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Associated morphology	Congenital absence	false	Inferred relationship	Some	1
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Finding site	Skin structure	false	Inferred relationship	Some	1
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Occurrence	Congenital	false	Inferred relationship	Some	2
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Finding site	Skin structure	false	Inferred relationship	Some	2
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Associated morphology	Congenital partial absence	false	Inferred relationship	Some	2
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Occurrence	Congenital	true	Inferred relationship	Some	1
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Associated morphology	Congenital absence	false	Inferred relationship	Some	1
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	Finding site	Skin part	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1771683015	Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn) (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
1782767017	Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)	en	Synonym	Active	Initial character case insensitive	SNOMED CT core